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Neurology|November 4, 2000
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophyK Vahedi, C Denier, A Ducros, et al.Annals of Neurology|March 1, 1995
A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19pK Vahedi, A Joutel, P Van Bogaert, et al.European Journal of Neurology|April 21, 2010
EFNS guideline on the treatment of cerebral venous and sinus thrombosis in adult patientsK Einhäupl, J Stam, M-G Bousser, et al.Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.The New England Journal of Medicine|December 1, 1994
Atherosclerotic disease of the aortic arch and the risk of ischemic strokeP Amarenco, A Cohen, C Tzourio, et al.European Journal of Neurology|June 27, 2006
EFNS guideline on the treatment of cerebral venous and sinus thrombosisK Einhäupl, M-G Bousser, S F T M de Bruijn, et al.Journal of Neurology|May 3, 2002
Efficacy and tolerability of acetazolamide in migraine prophylaxis: a randomised placebo-controlled trialK Vahedi, P Taupin, R Djomby, et al.The American Journal of Medicine|May 7, 1999
Oral anticoagulation in patients with atrial fibrillation: adherence with guidelines in an elderly cohortR H White, M A McBurnie, T Manolio, et al.Stroke|August 4, 2001
beta(2)-Glycoprotein 1-dependent anticardiolipin antibodies and risk of ischemic stroke and myocardial infarction: the honolulu heart programR L Brey, R D Abbott, J D Curb, et al.Pageof 31